S100-alarmins: potential therapeutic targets for arthritis

被引:37
作者
Austermann, Judith [1 ]
Zenker, Stefanie [1 ]
Roth, Johannes [1 ]
机构
[1] Univ Munster, Inst Immunol, Rontgenstr 21, D-48149 Munster, Germany
关键词
Alarmins; new diagnostic tools; rheumatoid arthritis; S100A8; S100A9; MYELOID-RELATED PROTEINS; JUVENILE IDIOPATHIC ARTHRITIS; FAMILIAL MEDITERRANEAN FEVER; CALCIUM-BINDING PROTEINS; MRP8/14; SERUM-LEVELS; RHEUMATOID-ARTHRITIS; SUPPRESSOR-CELLS; S100; PROTEINS; JOINT INFLAMMATION; DISEASE-ACTIVITY;
D O I
10.1080/14728222.2017.1330411
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: In arthritis, inflammatory processes are triggered by numerous factors that are released from joint tissues, promoting joint destruction and pathological progression. During inflammation, a novel family of pro-inflammatory molecules called alarmins is released, amplifying inflammation and joint damage.Areas covered: With regard to the role of the alarmins S100A8 and S100A9 in the pathogenesis of arthritis, recent advances and the future prospects in terms of therapeutic implications are considered.Expert opinion: There is still an urgent need for novel treatment strategies addressing the local mechanisms of joint inflammation and tissue destruction, offering promising therapeutic alternatives. S100A8 and S100A9, which are the most up-regulated alarmins during arthritis, are endogenous triggers of inflammation, defining these proteins as promising targets for local suppression of arthritis. In murine models, the blockade of S100A8/S100A9 ameliorates inflammatory processes, including arthritis, and there are several lines of evidence that S100-alarmins may already be targeted in therapeutic approaches in man.
引用
收藏
页码:739 / 751
页数:13
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